GABBROVET 140 MG/ML SOLUTION FOR USE IN DRINKING WATER, MILK OR MILK REPLACER FOR PRE-RUMINANT CATTLE AND PIGS
  • Paromomycin sulfate
  • Valid
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Product identification

Medicine name:
GABBROVET 140 MG/ML SOLUTION FOR USE IN DRINKING WATER, MILK OR MILK REPLACER FOR PRE-RUMINANT CATTLE AND PIGS
Active substance and strength:
  • Paromomycin sulfate
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA07AA06
Authorisation number:
  • V 915/18/05/1699
Product identification number:
  • a2e64dbe-2212-4ba5-8624-d6a54c0c226d
Permanent identification number:
  • 600000031098

Product details

Legal status of supply:
This information is not available for this product.
Pharmaceutical form:
  • Solution for use in drinking water
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        20
        day
    • Pig
      • Meat and offal
        3
        day

Availability

Package description:
  • Box of 1 vial of 250 mL
  • Box of 1 vial of 500 mL
  • Box of 1 vial of 1000 mL
  • Vial of 125 mL
  • Vial of 250 mL
  • Vial of 500 mL
  • Vial of 1000 mL
  • Box of 1 vial of 125 mL
Manufacturing sites for batch release:
This information is not available for this product.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.

Authorisation details

Authorisation status:
  • Valid
Authorisation procedure type:
  • Marketing Authorisation
Procedure number:
  • FR/V/0317/001
Date of authorisation status change:
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Authorisation country:
  • Luxembourg
Responsible authority:
  • DPM
Marketing authorisation holder:
  • Ceva Sante Animale
Marketing authorisation issued:
Reference member state:
  • France
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.

Additional information

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

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